Package 68788-8375-2

Brand: extra strength pain relief

Generic: acetaminophen
NDC Package

Package Facts

Identity

Package NDC 68788-8375-2
Digits Only 6878883752
Product NDC 68788-8375
Product ID 68788-8375_7ba209ec-3695-4163-8ca0-61c894fad3bf
Description

237 mL in 1 BOTTLE (68788-8375-2)

Marketing

Marketing Status
Marketed Since 2023-02-24
Brand extra strength pain relief
Generic acetaminophen
Sample Package No

Linked Drug Pages (1)

EXTRA STRENGTH PAIN RELIEF ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "7ba209ec-3695-4163-8ca0-61c894fad3bf", "openfda": {"unii": ["362O9ITL9D"], "spl_set_id": ["e18294f5-8fd5-4ac6-802c-f6d257e8bee7"], "manufacturer_name": ["Preferred Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "237 mL in 1 BOTTLE (68788-8375-2)", "package_ndc": "68788-8375-2", "marketing_start_date": "20230224"}], "brand_name": "EXTRA STRENGTH PAIN RELIEF", "product_id": "68788-8375_7ba209ec-3695-4163-8ca0-61c894fad3bf", "dosage_form": "SUSPENSION", "product_ndc": "68788-8375", "generic_name": "Acetaminophen", "labeler_name": "Preferred Pharmaceuticals Inc.", "product_type": "HUMAN OTC DRUG", "brand_name_base": "EXTRA STRENGTH PAIN RELIEF", "active_ingredients": [{"name": "ACETAMINOPHEN", "strength": "500 mg/15mL"}], "application_number": "343", "marketing_category": "OTC MONOGRAPH DRUG", "marketing_start_date": "20230224", "listing_expiration_date": "20261231"}